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Viscoelastic properties of collagen hydrogels

机译:胶原水凝胶的粘弹性

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Introduction: Because of their exceptional biological properties, reconstituted collagen gels are widely used as scaffolds even though their low elastic modulus (~ 500 Pa) limits their applications. The mechanical properties of collagen are governed by viscoelasticity. Unfortunately, few reports deal the mechanical properties of hydrogels that need to be addressed to understand the behavior of suchhydrogels when submitted to either creep-like or relaxation-like mechanical testing. Materials and Methods: Type Ⅰ collagen was extracted from rat-tail tendons and solubilized in acetic acid solution (0.02N) at 4 g/L as previously reported. Unconfined compression tests were made on disk shaped samples with a 25 mm compression plate attached to a 150 gf load cell mounted on a Biomomentum Mach 1 (Laval, Canada) testing apparatus. Compression tests were performed at room temperature in Phosphate-Buffered Saline (PBS) solution. Viscoelastic models based on two time constants Maxwell and standard linear solid were used. In addition, to reconcile experimental results and theory nonlinear stress-strain relationship based on Neo-Hookean and Mooney-Rivlin models were used. Results: Figure 1 shows a typical multiple relaxation test obtained with three samples: a water drop, a native collagen hydrogel and a collagen gel that has been colonized with smooth muscle cells for one week. The load of the water drop is increasingly oriented toward the tension side (negative) of the load curve due to increased surface tension force. The load curve of the native collagen gel is almost neutral and slightly toward the negative part. This indicates that the collagen native hydrogel exhibits no real residual stress when compressed for many steps. The viscoelastic model of such a material necessitates the use of Maxwell bodies. The other curve shows a residual stress that increases with the depth of the compression. In this case, the standard linear solid viscoelastic model is used. In figure 2, only the compression phase is illustrated. The simulation curves to reproduce the experimental result are indicated. Using a single Maxwell body, one can reproduce the experimental load if two conditions are met. The first condition requires a long time constant (~ 150s). As illustrated, a fast time constant is not adequate to reproduce the results. The second condition requires that a nonlinear relationship between Load and strain be used. In this case, a neo-hookean approach is used. Only in this combination of parameters, can one hope to reproduce experimental tests with simulation using standard viscoelastic models. Conclusion: This paper will present the results of many tests performed on collagen gels and present the conclusions regarding the viscoelastic models that should be retained when dealing with collagen gels mechanical properties.
机译:简介:由于其特殊的生物学性质,即使它们的低弹性模量(〜500Pa)限制了它们的应用,重构的胶原凝胶也被广泛用作支架。胶原蛋白的机械性能受粘弹性的控制。不幸的是,很少有报道涉及需要解决的水凝胶的机械性质,以了解在提交蠕变或放松的机械测试时理解如此的这种行为。材料和方法:Ⅰ型胶原从大鼠尾筋萃取,如前所述,在4g / L的乙酸溶液(0.02N)中溶解。在圆盘状样品上进行了非束缚的压缩试验,其中25mm压缩板连接到安装在生物传感马赫1(加拿大Laval,Canada)测试装置上的150 GF载荷单元上。在室温下在磷酸盐缓冲盐水(PBS)溶液中进行压缩试验。使用基于两个时间常数Maxwell和标准线性固体的粘弹性模型。此外,为了调和基于Neo-Hoxean和Mooney-Rivlin模型的实验结果和理论非线性应力 - 应变关系。结果:图1显示了用三个样品获得的典型多放松试验:水滴,天然胶原水凝胶和胶原凝胶,其已与平滑肌细胞沉积一周。由于表面张力增加,水滴的负荷越来越朝向负载曲线的张力侧(负)导致。天然胶原凝胶的载荷曲线几乎是中性的,并且略微向负部件略微中性。这表明胶原蛋白天然水凝胶在许多步骤压缩时没有真正的残余应力。这种材料的粘弹性模型需要使用Maxwell身体。另一曲线显示了随着压缩深度而增加的残余应力。在这种情况下,使用标准的线性固体粘弹性模型。在图2中,仅示出了压缩阶段。指出了再现实验结果的模拟曲线。如果满足两个条件,可以使用单个麦克斯韦全身,可以再现实验负载。第一个条件需要很长的时间常数(〜150s)。如图所示,快速时间常数不足以再现结果。第二条件要求使用负载和应变之间的非线性关系。在这种情况下,使用Neo-Hookean方法。只有在这种参数的组合中,可以希望使用标准粘弹性模型进行模拟再现实验测试。结论:本文将介绍对胶原凝胶对胶原凝胶进行的许多测试的结果,并在处理胶原凝胶机械性能时应保留的粘弹性模型的结论。

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